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Updated: May 13, 2026

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初级乳性失动症基因变异的异质性:俄罗斯的一个遗传数据库分析

Elena I Kondratyeva1, Sergey N Avdeev2, Tatiana A Kyian1

  • 1Research Centre for Medical Genetics, 1 Moskvorechye St., Moscow 115522, Russia.

International journal of molecular sciences
|December 11, 2025
PubMed
概括

在俄罗斯进行的原发性纤维动力障碍 (PCD) 遗传分析显示,DNAH5和DNAH11基因中存在常见变异. 确定了新的变异,DNAH5与卡塔根纳综合征有关.

关键词:
我们的数据库数据库数据库数据库.诊断 诊断 诊断 诊断 诊断分子遗传测试 分子遗传测试主要的状动力障碍症.测序的测序是指测序的测序.

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